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Single Bolus Recombinant Nonimmunogenic Staphylokinase (Fortelyzin) and Bolus Infusion Alteplase in Patients With AIS

Primary Purpose

Ischemic Stroke

Status
Completed
Phase
Phase 3
Locations
Russian Federation
Study Type
Interventional
Intervention
Recombinant staphylokinase
Alteplase
Sponsored by
Supergene, LLC
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Ischemic Stroke focused on measuring Acute Ischemic Stroke, Fibrinolysis, Fortelyzin

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Men and women between the ages of 18 and 80 (Version 1.0)
  • Men and women aged 18 years and older, after 80 years with caution (Version 2.0)
  • Verified diagnosis of ischemic stroke (from 5 to 25 points on the NIHSS scale). (Version 1.0)
  • Verified diagnosis of ischemic stroke (Version 2.0)
  • The time from the onset of the disease is no more than 4.5 hours.
  • Informed consent received

Exclusion Criteria:

  • The time of the onset of the first symptoms is more than 4.5 hours from the onset of the disease or the time of the onset of the first symptoms of a stroke is not known (for example, the development of a stroke during sleep - the so-called "night stroke").
  • Increased sensitivity to alteplase, gentamicin (residual traces from the production process).
  • Systolic blood pressure above 185 mm Hg. Art. Or diastolic blood pressure above 110 mm Hg. Art. Or the need for / in the administration of drugs to reduce blood pressure to these boundaries.
  • Neuroimaging (CT, MRI) signs of intracranial hemorrhage, brain tumors, arteriovenous malformation, brain abscess, aneurysm of cerebral vessels.
  • Surgery on the brain or spinal cord.
  • Suspicion of subarachnoid hemorrhage.
  • Signs of severe stroke: clinical signs (stroke scale NIH> 25), neuroimaging (according to CT of the brain and / or MRI of the brain in the DWI, the ischemia focuses on the territory of more than 1/3 of the CMA pool).
  • Simultaneous reception of oral anticoagulants, for example, warfarin with INR> 1.3.
  • The use of direct anticoagulants (heparin, heparinoids) in the preceding stroke of 48 h with APTT values above the norm.
  • Prior stroke or severe head injury within 3 months.
  • Significant regression of neurological symptoms during the observation of the patient.(Version 1.0)
  • Light neurological symptoms (NIH <4 points). (Version 1.0)
  • Significant regression of neurological symptoms during the observation of the patient before thrombolisis (Version 2.0)
  • Hemorrhagic stroke or stroke, unspecified in history.
  • Strokes of any genesis in the history of a patient with diabetes mellitus.
  • Gastrointestinal bleeding or bleeding from the genitourinary system in the last 3 weeks. Confirmed exacerbations of gastric ulcer and duodenal ulcer during the last 3 months.
  • Extensive bleeding now or within the previous 6 months.
  • Severe liver disease, including liver failure, cirrhosis, portal hypertension (with varicose veins of the esophagus), active hepatitis.
  • Acute pancreatitis.
  • Bacterial endocarditis, pericarditis.
  • Aneurysms of arteries, malformations of arteries and veins. Suspicion of exfoliating aortic aneurysm.
  • Neoplasms with an increased risk of bleeding.
  • Large operations or severe injuries within the last 14 days, minor surgery or invasive manipulation in the last 10 days.
  • Puncture of uncompensated arteries and veins during the last 7 days.
  • Prolonged or traumatic cardiopulmonary resuscitation (more than 2 min).
  • Pregnancy, obstetrics, 10 days after birth.
  • The number of platelets is less than 100,000 / μL.
  • Blood glucose less than 2.7 mmol / l or more than 22.0 mmol / l.
  • Hemorrhagic diathesis, including renal and hepatic insufficiency.
  • Data on bleeding or acute trauma (fracture) at the time of examination.
  • Seizures in the onset of the disease, if there is no certainty that the seizure is a clinical manifestation of ischemic stroke with a postictal residual deficiency.

Sites / Locations

  • Regional Clinical Hospital
  • St.Iosaf's Belgorod Regional Clinical Hospital
  • Regional Clinical Hospital №3
  • Regional Clinical Hospital №1
  • Regional Clinical Hospital
  • Regional Clinical Hospital
  • Ochapowski Regional Hospital №1
  • Regional Clinical Hospital
  • Regional Clinical Hospital
  • Regional Clinical Hospital
  • City Clinical Hospital №11
  • Regional Clinical Hospital
  • Regional Clinical Hospital
  • Regional Clinical Hospital
  • Regional Clinical Hospital
  • Regional Clinical Hospital
  • City Clinical Hospital of Emergency №25
  • Regional Clinical Hospital №1

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Recombinant staphylokinase

Actilyse

Arm Description

Lyophilizate for solution making for intravenous injection, 5 mg (745000 ME). 10 mg of drug reconstituted in 10 ml of 0.9% solution of NaCl given as single i.v. bolus over 5 - 10 seconds

Intravenous alteplase 0.9 mg/kg (10% bolus and 90% as IV infusion over 1 hour, maximum 90 mg)

Outcomes

Primary Outcome Measures

Good functional recovery
Good functional recovery on the 90th day (modified Rankin scale, 0-1 point).

Secondary Outcome Measures

Modified Rankin scale (0-1) + NIHSS (0-1) + Barthel (95-100)
Composite endpoint
NIHSS
NIHSS after 24 hours
NIHSS
NIHSS after 90 days
All Cause Death
Death caused by any event
Hemorrhagic transformation
Hemorrhagic transformation (all cases).
Symptomatic hemorrhagic transformation
Increase in NIHSS index by 4 points or more or death
Serious adverse reactions and adverse reactions
Serious adverse reactions and adverse reactions (all cases)

Full Information

First Posted
May 10, 2017
Last Updated
December 11, 2020
Sponsor
Supergene, LLC
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1. Study Identification

Unique Protocol Identification Number
NCT03151993
Brief Title
Single Bolus Recombinant Nonimmunogenic Staphylokinase (Fortelyzin) and Bolus Infusion Alteplase in Patients With AIS
Official Title
Multicenter Open Label Randomized Comparative Study of Efficacy and Safety of Single Bolus Injection of Recombinant Nonimmunogenic Staphylokinase (Fortelyzin) and Bolus Infusion Alteplase (Actilyse) in Patients With Acute Ischemic Stroke
Study Type
Interventional

2. Study Status

Record Verification Date
September 2020
Overall Recruitment Status
Completed
Study Start Date
March 18, 2017 (Actual)
Primary Completion Date
March 23, 2019 (Actual)
Study Completion Date
June 20, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Supergene, LLC

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The aim of the study is to determine if single-bolus recombinant nonimmunogenic staphylokinase is effective and save thrombolytic agent in patients with ischemic stroke in comparison to alteplase.
Detailed Description
Experimental Drug Profile. The active substance of Fortelyzin is Forteplase. It's recombinant protein which contains aminoacid sequence of staphylokinase. It is single chain molecula, consists of 138 aminoacids, weight 15.5 kDa. When staphylokinase is added to human plasma containing a fibrin clot, it preferentially reacts with plasmin at the clot surface, forming a plasmin-staphylokinase complex. This complex activates plasminogen trapped in the thrombus. The plasmin-staphylokinase complex and plasmin bound to fibrin are protected from inhibition by alpha2-antiplasmin. Once liberated from the clot (or generated in plasma), however, they are rapidly inhibited by alpha2-antiplasmin. This selectivity of action confines the process of plasminogen activation to the thrombus, preventing excessive plasmin generation, alpha2-antiplasmin depletion, and fibrinogen degradation in plasma. In rabbits anti forteplase antibodies are not produced. It was achieved by replacement of amino acids in immunogenic epitop of molecule staphylokinase. Blood fibrinogen decrease after i.v. injection of Fortelyzin less 10% within first 24 hours. Angiographic data suggests that restoration of coronary blood flow appears in up to 80% of patients with STEMI after i.v. injection of Fortelyzin. Main goals of the study are to prove an efficacy of the single-bolus intravenous injection of recombinant nonimmunogenic staphylokinase (Fortelyzin) in comparison with bolus infusion alteplase(Actilyse) in patients with ischemic stroke. To prove a safety and to assess possible adverse events in the single-bolus intravenous injection of recombinant nonimmunogenic staphylokinase (Fortelyzin) in comparison with bolus infusion alteplase (Actilyse) in patients with ischemic stroke. Study Design. All eligible patients will be randomized in two equal groups for administration recombinant nonimmunogenic staphylokinase (Fortelyzin) or alteplase (Actilyse) by using "envelope method" of randomization. It is an open-lable study. Each of agents will be administered no longer then 4,5 hours from symptoms onset. Comparative agent will be administered as prescribed in its instructions. All patients will be examination for 90 days

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Ischemic Stroke
Keywords
Acute Ischemic Stroke, Fibrinolysis, Fortelyzin

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Model Description
All eligible patients will be randomized in two equal groups for administration recombinant nonimmunogenic staphylokinase (Fortelyzin) or alteplase (Actilyse) by using "envelope method" of randomization. It is an open-lable study. Each of agents will be administered no longer then 4,5 hours from symptoms onset. Comparative agent will be administered as prescribed in its instructions. All patients will be examination for 90 days
Masking
None (Open Label)
Masking Description
All eligible patients will be randomized in two equal groups for administration recombinant nonimmunogenic staphylokinase (Fortelyzin) or alteplase (Actilyse) by using "envelope method" of randomization.
Allocation
Randomized
Enrollment
336 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Recombinant staphylokinase
Arm Type
Experimental
Arm Description
Lyophilizate for solution making for intravenous injection, 5 mg (745000 ME). 10 mg of drug reconstituted in 10 ml of 0.9% solution of NaCl given as single i.v. bolus over 5 - 10 seconds
Arm Title
Actilyse
Arm Type
Active Comparator
Arm Description
Intravenous alteplase 0.9 mg/kg (10% bolus and 90% as IV infusion over 1 hour, maximum 90 mg)
Intervention Type
Drug
Intervention Name(s)
Recombinant staphylokinase
Other Intervention Name(s)
Fortelyzin
Intervention Description
10 mg of drug reconstituted in 10 ml of 0.9% solution of NaCl given as single i.v. bolus over 5 - 10 seconds
Intervention Type
Drug
Intervention Name(s)
Alteplase
Other Intervention Name(s)
Actilyse
Intervention Description
Intravenous alteplase 0.9 mg/kg (10% bolus and 90% as IV infusion over 1 hour, maximum 90 mg)
Primary Outcome Measure Information:
Title
Good functional recovery
Description
Good functional recovery on the 90th day (modified Rankin scale, 0-1 point).
Time Frame
within 90 days after fibrinolysis
Secondary Outcome Measure Information:
Title
Modified Rankin scale (0-1) + NIHSS (0-1) + Barthel (95-100)
Description
Composite endpoint
Time Frame
within 90 days after fibrinolysis
Title
NIHSS
Description
NIHSS after 24 hours
Time Frame
after 24 hours
Title
NIHSS
Description
NIHSS after 90 days
Time Frame
within 90 days after fibrinolysis
Title
All Cause Death
Description
Death caused by any event
Time Frame
within 90 days after fibrinolysis
Title
Hemorrhagic transformation
Description
Hemorrhagic transformation (all cases).
Time Frame
within 90 days after fibrinolysis
Title
Symptomatic hemorrhagic transformation
Description
Increase in NIHSS index by 4 points or more or death
Time Frame
within 90 days after fibrinolysis
Title
Serious adverse reactions and adverse reactions
Description
Serious adverse reactions and adverse reactions (all cases)
Time Frame
within 90 days after fibrinolysis

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Men and women between the ages of 18 and 80 (Version 1.0) Men and women aged 18 years and older, after 80 years with caution (Version 2.0) Verified diagnosis of ischemic stroke (from 5 to 25 points on the NIHSS scale). (Version 1.0) Verified diagnosis of ischemic stroke (Version 2.0) The time from the onset of the disease is no more than 4.5 hours. Informed consent received Exclusion Criteria: The time of the onset of the first symptoms is more than 4.5 hours from the onset of the disease or the time of the onset of the first symptoms of a stroke is not known (for example, the development of a stroke during sleep - the so-called "night stroke"). Increased sensitivity to alteplase, gentamicin (residual traces from the production process). Systolic blood pressure above 185 mm Hg. Art. Or diastolic blood pressure above 110 mm Hg. Art. Or the need for / in the administration of drugs to reduce blood pressure to these boundaries. Neuroimaging (CT, MRI) signs of intracranial hemorrhage, brain tumors, arteriovenous malformation, brain abscess, aneurysm of cerebral vessels. Surgery on the brain or spinal cord. Suspicion of subarachnoid hemorrhage. Signs of severe stroke: clinical signs (stroke scale NIH> 25), neuroimaging (according to CT of the brain and / or MRI of the brain in the DWI, the ischemia focuses on the territory of more than 1/3 of the CMA pool). Simultaneous reception of oral anticoagulants, for example, warfarin with INR> 1.3. The use of direct anticoagulants (heparin, heparinoids) in the preceding stroke of 48 h with APTT values above the norm. Prior stroke or severe head injury within 3 months. Significant regression of neurological symptoms during the observation of the patient.(Version 1.0) Light neurological symptoms (NIH <4 points). (Version 1.0) Significant regression of neurological symptoms during the observation of the patient before thrombolisis (Version 2.0) Hemorrhagic stroke or stroke, unspecified in history. Strokes of any genesis in the history of a patient with diabetes mellitus. Gastrointestinal bleeding or bleeding from the genitourinary system in the last 3 weeks. Confirmed exacerbations of gastric ulcer and duodenal ulcer during the last 3 months. Extensive bleeding now or within the previous 6 months. Severe liver disease, including liver failure, cirrhosis, portal hypertension (with varicose veins of the esophagus), active hepatitis. Acute pancreatitis. Bacterial endocarditis, pericarditis. Aneurysms of arteries, malformations of arteries and veins. Suspicion of exfoliating aortic aneurysm. Neoplasms with an increased risk of bleeding. Large operations or severe injuries within the last 14 days, minor surgery or invasive manipulation in the last 10 days. Puncture of uncompensated arteries and veins during the last 7 days. Prolonged or traumatic cardiopulmonary resuscitation (more than 2 min). Pregnancy, obstetrics, 10 days after birth. The number of platelets is less than 100,000 / μL. Blood glucose less than 2.7 mmol / l or more than 22.0 mmol / l. Hemorrhagic diathesis, including renal and hepatic insufficiency. Data on bleeding or acute trauma (fracture) at the time of examination. Seizures in the onset of the disease, if there is no certainty that the seizure is a clinical manifestation of ischemic stroke with a postictal residual deficiency.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Evgenii I Gusev, MD, PhD
Organizational Affiliation
Pirogov Russian National Research Medical University
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Sergey S Markin, MD, PhD
Organizational Affiliation
Supergene, LLC
Official's Role
Study Director
Facility Information:
Facility Name
Regional Clinical Hospital
City
Barnaul
ZIP/Postal Code
656024
Country
Russian Federation
Facility Name
St.Iosaf's Belgorod Regional Clinical Hospital
City
Belgorod
ZIP/Postal Code
308007
Country
Russian Federation
Facility Name
Regional Clinical Hospital №3
City
Chelyabinsk
ZIP/Postal Code
454021
Country
Russian Federation
Facility Name
Regional Clinical Hospital №1
City
Ekaterinburg
ZIP/Postal Code
620014
Country
Russian Federation
Facility Name
Regional Clinical Hospital
City
Irkutsk
ZIP/Postal Code
664079
Country
Russian Federation
Facility Name
Regional Clinical Hospital
City
Kaluga
ZIP/Postal Code
248007
Country
Russian Federation
Facility Name
Ochapowski Regional Hospital №1
City
Krasnodar
ZIP/Postal Code
350086
Country
Russian Federation
Facility Name
Regional Clinical Hospital
City
Kursk
ZIP/Postal Code
305007
Country
Russian Federation
Facility Name
Regional Clinical Hospital
City
Nizhny Novgorod
ZIP/Postal Code
603126
Country
Russian Federation
Facility Name
Regional Clinical Hospital
City
Orenburg
ZIP/Postal Code
460018
Country
Russian Federation
Facility Name
City Clinical Hospital №11
City
Ryazan'
ZIP/Postal Code
390000
Country
Russian Federation
Facility Name
Regional Clinical Hospital
City
Ryazan
ZIP/Postal Code
390039
Country
Russian Federation
Facility Name
Regional Clinical Hospital
City
Samara
ZIP/Postal Code
443095
Country
Russian Federation
Facility Name
Regional Clinical Hospital
City
Sankt-peterburg
ZIP/Postal Code
194291
Country
Russian Federation
Facility Name
Regional Clinical Hospital
City
Tver
ZIP/Postal Code
170036
Country
Russian Federation
Facility Name
Regional Clinical Hospital
City
Ulyanovsk
ZIP/Postal Code
432017
Country
Russian Federation
Facility Name
City Clinical Hospital of Emergency №25
City
Volgograd
ZIP/Postal Code
400138
Country
Russian Federation
Facility Name
Regional Clinical Hospital №1
City
Voronezh
ZIP/Postal Code
394066
Country
Russian Federation

12. IPD Sharing Statement

Plan to Share IPD
No
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URL
http://eurheartj.oxfordjournals.org/content/early/2014/09/10/eurheartj.ehu278
Description
ESC/EACTS Guidelines in Myocardial Revascularisation
URL
http://eurheartj.oxfordjournals.org/content/ehj/33/20/2569.full.pdf
Description
ESC Guidelines for the management of acute myocardial infarction in patients presenting with ST-segment elevation
URL
http://www.ich.org/products/guidelines/efficacy/article/efficacy-guidelines.html
Description
Efficacy Guidelines. The work carried out by ICH under the Efficacy heading is concerned with the design, conduct, safety and reporting of clinical trials.
URL
http://elibrary.ru/item.asp?id=36518074
Description
FORTELYZIN® IN COMPARISON WITH METALYSE® FOR ST-ELEVATED MYOCARDIAL INFARCTION: ONE-YEAR RESULTS AND CLINICAL OUTCOMES OF A MULTICENTER RANDOMIZED STUDY FRIDOM1
URL
http://elibrary.ru/item.asp?id=30575583
Description
FORTELYZIN® VERSUS METALYSE® IN ST-SEGMENT ELEVATION MYOCARDIAL INFARCTION: RESULTS OF MULTICENTER RANDOMIZED trial FRIDOM 1
URL
http://elibrary.ru/item.asp?id=32488266
Description
Neurology: national guidelines

Learn more about this trial

Single Bolus Recombinant Nonimmunogenic Staphylokinase (Fortelyzin) and Bolus Infusion Alteplase in Patients With AIS

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